LRTI Flashcards

1
Q

host interventions that can increase likelihood of infection

A

smoking
alcohol
altered level of consciousness
endotracheal tube

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2
Q

host disease states increasing risk of infection

A

immunosupression
diabetes
asplenia
elderly

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3
Q

pathogen mediated ways infections can happen

A

surface adhesions
pili
exotoxins
enzymes

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4
Q

define community acquired pneumonia

A

pneumonia that developed outside the hospital or within first 48 hours of hospital admission

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5
Q

what is the most common cause of infection related hospitalization and mortality in the US

A

CAP

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6
Q

what is the most common pathway for bacteria pneumonia

A

aspiration

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7
Q

when does aspiration happen

A

during sleep
disorders that impair consciousness and depress gag reflex

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8
Q

what are the three ways that infection can happen

A

aspiration
aerosolization
bloodborne

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9
Q

what microorganism class is the most common pathogenic organism for CAP

A

virus

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10
Q

common bacterial pathogens of CAP

A

strep pneumoniae
haemophilus influenza
mycoplasma pneumoniae
legionella pneumophila
chlaymydia pneumoniae
staph aureus

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11
Q

which bacterial organism is most common in CAP?

A

strep pneumo

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12
Q

risk factors for drug resistance to strep

A

< 6 years
> 65 years
prior antibiotic therapy
co-morbid conditions
close quarters

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13
Q

how is mycoplasma pneumoniae spread

A

person to person contact

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14
Q

mycoplasma pneumoniae symptoms

A

2-3 week incubation period, slow onset of symptoms
cough, fever, headache, sore throat, N/V

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15
Q

what may we see with imaging in someone with mycoplasma

A

patchy interstitial infiltrates

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16
Q

what are the atypical pathogens for CAP?

A

legionella
mycoplasma
chlamydia

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17
Q

how is legionella spread

A

aerosolization

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18
Q

who is at increased risk of legionella?

A

older males, chronic bronchitis, smokers, immunocompromsied

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19
Q

legionella characteristics and symptoms

A

multisystem involvement - high fevers, bradycardia, multi-lobar involvement, mental status change, LFT increase

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20
Q

staph aureus prevalence in CAP

A

low prevalence

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21
Q

risk factors for MRSA

A

2-14 days post flu
previous MRSA infection
previous hospitalization
previous use of IV antibiotics

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22
Q

what should we get if starting someone on empiric MRSA therapy?

A

MRSA nasal PCR - helps us rule OUT MRSA, doesn’t diagnose but tells us we don’t have

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23
Q

alcoholism organism risk

A

strep pneumo
anaerobes
klebsiella pneumonia

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24
Q

COPD/smoker risk pathogens

A

h flu, strep pneumo, moraxella, legionella

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25
Q

post influenza pneumonia risk pathogens

A

strep pneumo
staph aureus
h flu

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26
Q

structural lung disease risk pathogens

A

pseudomonas aeruginosa
staph aureus

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27
Q

recent antibiotic exposure risk pathogens

A

staph
pseudomonas

28
Q

which pathogens have a slower onset of symptoms in CAP

A

mycoplasma
chlamydia

29
Q

how might CAP symptoms be different in elderly?

A

no fever
decrease in functional status, weakness, mental status changes

30
Q

vitals associated with CAP

A

fever >38
HR > 90
SBP <90
RR >20

31
Q

CAP presentation on Xray bacterial

A

dense lobar infiltrates
consolidation

32
Q

CAP presentation on XRAY viral or atypical

A

patchy, diffuse interstitial infiltrates

33
Q

what quality of samples can we evaluate

A

> 25 PMNs
<10 epithelial cells

34
Q

testing we should get in CAP

A

could get resp culture - more used in HAP
blood culture
WBC
SCr,BUN, LFTs
O2 sat
Urinary antigen tests
nasopahyngeal PCR swab

35
Q

what do we use urinary antigen tests for

A

strep penumoniae
legionella pneumophila
(helpful in getting a positive but we don’t change therapy)

36
Q

what do we use nasopharyngeal PCR swabs for

A

MRSA and viral tests

37
Q

when do we get a respiratory culture and a blood culture?

38
Q

severe CAP major criteria (1)

A

septic shock
mechanical ventillation

39
Q

severe CAP minor criteria (3)

A

RR >30
multilobar infiltrates
confusion/disorientation
BUN >20
WBC < 4,000
Platelet < 100,000
temp <36
hypotension requiring fluids

40
Q

procalcitonin used for what

A

guides duration of treatment
not useful for starting therapy

41
Q

supportive measures used in CAP

A

humidified oxygen
bronchodilators
fluids
chest physiotherapy

42
Q

empiric CAP outpatient therapy - no comorbidities

A

amoxicillin
doxycycline
- azithromycin if <25% resist

43
Q

empiric CAP outpatient therapy - comorbidities

A

beta lactam + macrolide/doxy
- amox/clav
- cefpodoxime
- cefuroxime

44
Q

empiric CAP inpatient therapy - non-severe (no pseudomonas or MRSA risk)

A

beta lactam + macrolide
- ampicillin/sulbactam
- ceftriaxone
- doxy if contraindicated
levofloxacin
moxifloxacin

45
Q

empiric CAP inpatient therapy severe (no pseudomonas or MRSA risk)

A

beta lactam + macrolide (FQ np)
- ampicillin/sulbactan
- ceftriaxone
- doxy if contraindicated

46
Q

empiric CAP MRSA risk factors

A

2-14 days post influenza
previous MRSA infection
previous hospitalization w use of IV antibiotics within last 90 days

47
Q

empiric CAP MRSA coverage to add

A

linezolid
vancomycin

48
Q

empiric CAP pseudomonas risk factors

A

previous pseudomonas inf
previous hosp and IV antibiotic use within last 90 days

49
Q

empiric CAP pseudomonas coverage agents

A

piperacillin/tazobactam
cefepime
meropenem

50
Q

are corticosteroids reccommended in CAP?

A

no, only if septic shock

51
Q

how long should we continue CAP therapy?

A

5 days minimum

52
Q

clinical stability factors for discontinuation of antibiotics

A

temp <38 for 24 hrs
HR <100
RR <24
SBP >90
O2 sat >90
baseline mental status

53
Q

what is HAP and VAP

A

occurring > 48 hours post admission and for VAP after endotracheal intubation

54
Q

pathogenesis of HAP

A

miro aspirations of secretions, usually 3-5 days after hospitalization and coverts to gram negative organisms
aspiration GI contents
blood source
direct inoculation via intubation
mechanical vent

55
Q

presentation of HAP/VAP

A

new lung infiltrate or new onset of fever, purulent sputum, leukocytosis

56
Q

common pathogens for HAP/VAP

A

pseudomonas
enteric gram negative bacilli
acinetobacter
staph aureus (MRSA

57
Q

microbiology testing done in HAP/VAP

A

respiratory culture
blood culture

58
Q

invasive respiratory culture threshold for sample

A

specimen brush <10^3 CFU
BAL: < 10^4

59
Q

risk factors for MDR VAP

A

prior IV antibiotic use within 90 days
septic shock at time of dx
ARDS prior to dx
acute renal replacement therapy
> 5 days hospitalization

60
Q

when to cover MRSA HAP

A

risk factors
ICUs where > 10% MRSA isolates

61
Q

MRSA coverage treatment for HAP

A

linezolid
vancomycin

62
Q

pseudomonas coverage treatment for HAP

A

piperacillin/tazobactam
meropenem
imipenem
levofloxacin
cefepime

63
Q

empiric HAP - not at high risk for mortality (not on vent or septic shock)

A

piperacillin/tazobactam
meropenem
imipenem
levofloxacin
cefepime
one of those

PLUS MRSA (if risk)
linezolid
vanc

64
Q

empiric HAP - high risk for mortality (septic shock or vent)

A

piperacillin/tazobactam
meropenem
imipenem
levofloxacin
cefepime
tobramycin/amikacin
2 of those in diff classes
plus vanc or linezolid

65
Q

duration of therapy for HAP and VAP

A

7 days minimum if clinically stable

66
Q

VAP - does longer therapy decrease mortality?

A

no, 7 days is good